Canonical Allele Identifier: CA519345335
Gene: ABCD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.152991615C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153726160C>G , CM000685.2:g.153726160C>G GRCh38
NC_000023.10:g.152991615C>G , CM000685.1:g.152991615C>G GRCh37
NC_000023.9:g.152644809C>G NCBI36
NG_009022.2:g.6293C>G
NG_023231.1:g.3587G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218104.6:c.894C>G MANE Select ENSP00000218104.3:p.Gly298=
ENST00000218104.5:c.894C>G ENSP00000218104.3:p.Gly298=
ENST00000370129.4:c.339C>G ENSP00000359147.3:p.Gly113=
NM_000033.3:c.894C>G NP_000024.2:p.Gly298=
XR_938507.1:n.1310C>G
XR_938507.2:n.1310C>G
NM_000033.4:c.894C>G MANE Select NP_000024.2:p.Gly298=
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